EP0494089B1 - Connecteur pour bouteille d'aspiration de fluides de blessures - Google Patents

Connecteur pour bouteille d'aspiration de fluides de blessures Download PDF

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Publication number
EP0494089B1
EP0494089B1 EP92104631A EP92104631A EP0494089B1 EP 0494089 B1 EP0494089 B1 EP 0494089B1 EP 92104631 A EP92104631 A EP 92104631A EP 92104631 A EP92104631 A EP 92104631A EP 0494089 B1 EP0494089 B1 EP 0494089B1
Authority
EP
European Patent Office
Prior art keywords
membrane
connection device
central opening
face
hollow cylinder
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP92104631A
Other languages
German (de)
English (en)
Other versions
EP0494089A1 (fr
Inventor
Helmut Dr. Rer. Nat. Fell
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
MEDINORM AG medizintechnische Produkte
Original Assignee
MEDINORM AG medizintechnische Produkte
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from DE3724483A external-priority patent/DE3724483C2/de
Priority claimed from DE8714456U external-priority patent/DE8714456U1/de
Application filed by MEDINORM AG medizintechnische Produkte filed Critical MEDINORM AG medizintechnische Produkte
Publication of EP0494089A1 publication Critical patent/EP0494089A1/fr
Application granted granted Critical
Publication of EP0494089B1 publication Critical patent/EP0494089B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/71Suction drainage systems
    • A61M1/73Suction drainage systems comprising sensors or indicators for physical values
    • A61M1/732Visual indicating means for vacuum pressure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/64Containers with integrated suction means
    • A61M1/66Pre-evacuated rigid containers, e.g. Redon bottles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/71Suction drainage systems
    • A61M1/74Suction control
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/71Suction drainage systems
    • A61M1/74Suction control
    • A61M1/743Suction control by changing the cross-section of the line, e.g. flow regulating valves
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/58Means for facilitating use, e.g. by people with impaired vision
    • A61M2205/583Means for facilitating use, e.g. by people with impaired vision by visual feedback
    • A61M2205/584Means for facilitating use, e.g. by people with impaired vision by visual feedback having a color code

Definitions

  • the invention relates to a connection device for a Suction bottle for sucking off wound fluids during wound drainage.
  • a pre-evacuated feeding bottle is preferred with vacuum indicator, via a connecting hose with a perforated wound drainage tube connected in an airtight, closed wound cavity is inserted.
  • connection device usually used is a bare hose, with one end on a connecting piece on the feeding bottle and with his other End connected to a connector on the wound drainage tube becomes.
  • a clamping device is used to interrupt the connection device.
  • a generic connecting device of the beginning mentioned type is known from FR-A-2208545.
  • the Connection device has a breakthrough circular cylindrical body screwed onto a bottle can be. Wound fluids can enter the bottle be sucked in.
  • the required vacuum in the bottle can be regulated by means of a membrane.
  • the Membrane is circumferentially through the free, peripheral edge of a circular cylindrical hollow cylinder closed on one side pressed tightly against the cylindrical body.
  • the membrane is in the space between the pistons and present in the body. Unless the piston from the membrane is moved away, forms in the space between the piston and Membrane a differently large negative pressure.
  • the invention has for its object a connection device to specify for a feeding bottle that simple is designed and the problem-free replacement of a connected suction bottle allowed.
  • connection device is technically simple designed. Because completely through the membrane closed central opening at least one more no further opening through the membrane at the same time is closed, for example wound fluid can still flow into the connection device and, for example drain into an overflow vessel. The drainage of wound fluid so there is no need to interrupt from a wound, if a suction bottle filled with wound fluid against a new feeding bottle is to be replaced.
  • connection device is thus as Suction regulators trained by their Membrane depending on the on their interior and Pressures acting a central opening in an outer surface Membrane carrier releases or closes.
  • the pressure on the The outside can be adjusted in that the membrane carrier sealed with membrane in a hollow cylinder which is closed at the end on which Side of the membrane.
  • the back and forth is preferably carried out Pushing the membrane over by a rotary movement a screw thread between membrane support and hollow cylinder is led.
  • the end wall has of the hollow cylinder centrally an elastic sealing part which then presses on the membrane when the membrane carrier completely moved to the closed end of the hollow cylinder is what causes the membrane to the central opening in the Presses the membrane carrier and closes it. That’s it possible the connection between a feeding bottle attached to the central opening is connected, and the wound drainage tube to interrupt.
  • connection with central opening for the feeding bottle and the connection for the wound drainage tube has the membrane carrier preferably still further connections, namely for a vacuum indicator and / or for an overflow vessel, the central opening continues to flow into the wound secretion is closed.
  • a plurality of openings can also be present on a connection device in which the membrane is not slidable in the hollow cylinder, like this e.g. B. described in German patent application 37 24 483 is.
  • connection device 50 has a hollow cylinder 51 on one side through an end wall 52 is closed. Runs in the hollow cylinder 51 Membrane support 53 with a membrane 54 on the membrane support is attached, which is directed against the end wall 52 and which seals against the hollow cylinder 51. The move the membrane carrier 53 takes place via a screw connection, which is formed by two pins 55 on the membrane carrier 53, through two helical recesses 56 in the hollow cylinder 51 grab.
  • the membrane carrier 53 is designed so that it is on the front side, to which the membrane is attached, a circumferential Bead 57 has. One ends centrally in this end face Central opening 58, with a shut-off nozzle leading to the outside 24 communicates. Because the bead 57 is present is, close this, the mentioned end face 59 of the Membrane carrier 53 and the inside of the membrane 54 one Cavity 60, which is accessible through the central opening 58 for as long is as long as the membrane 54 is not so far against the end face 59 is deformed so that it is the central opening 58 closes.
  • the openings of three other sockets namely one Inlet nozzle 23, a vacuum indicator nozzle 61 and one Overflow nozzle 62.
  • the associated openings are an inlet opening 63, a measuring opening 64 or an overflow opening 65.
  • a vacuum indicator is on the vacuum indicator connector 61 and an overflow vessel to the overflow nozzle 62 connected. Both devices should be small-volume so that a vacuum quickly builds up in them.
  • the inlet port 23 is with a perforated wound drainage tube in connection and the shut-off nozzle 24 is on a feeding bottle connected.
  • the connection is made in a position of the connection device in which the membrane carrier 53 close to the end wall 52 of the hollow cylinder 51 stands so that an elastic sealing member 66, which is on the inside the end wall 52 is attached, the membrane 54 against the central opening 58 presses. Now becomes the hollow cylinder 51 screwed to the membrane carrier 53 moves its end wall 52 away from the membrane 54, whereby a negative pressure builds up in the space in between.
  • the pressure in the cavity 60 at which the membrane 54 from the central opening 58 takes off not only depends on the pressure on the Outside of membrane 54 and the pressure at the central opening 58 from, but also from the elastic force acting on the membrane 54 pulled over the bead 57 is exerted.
  • the extent of the negative pressure in the cavity 60 can thus be determined preselect the default of this elastic force and by the Moving the hollow cylinder 51 and membrane carrier 53 against each other fine tune.
  • the elastic force can influence the material of the membrane 54 or its Form can be taken or the height of the bead 57 and its height Inner diameter can be varied.
  • the adjustability serves between Hollow cylinder 51 and membrane supports 53 for fine adjustment a desired negative pressure.
  • membrane carrier 53 and hollow cylinder 51 can be made using any sliding construction. So instead of pegs that reach through recesses there are also shorter cones that are single [i in helical grooves in the inner peripheral wall of the Intervene in the hollow cylinder. Any other screw connection you can choose between hollow cylinder and membrane support. Locking connections can also be used where fixing in a new position after moving through Locking forces.

Landscapes

  • Health & Medical Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Hematology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • External Artificial Organs (AREA)
  • Manipulator (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Hooks, Suction Cups, And Attachment By Adhesive Means (AREA)
  • Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)

Claims (8)

  1. Dispositif de raccordement pour une bouteille d'aspiration servant à aspirer des liquides issus de plaies, qui est réalisé comme un dispositif de réglage d'aspiration, comprenant
    une membrane (54),
    un porte-membrane (53) de forme cylindrique circulaire, dont la face d'extrémité supérieure (59) est recouverte par la membrane (54), avec préservation d'une capacité (60), face d'extrémité dans laquelle débouche un orifice central (58) et dans laquelle est formé un orifice d'admission (63) pour les liquides provenant de plaies,
    ainsi qu'un cylindre circulaire creux (51) fermé en haut par une paroi de fermeture (52) et à l'intérieur duquel la membrane (54) est déplaçable et guidée en va-et-vient en direction longitudinale, en étant étanchée vis-à-vis de la paroi interne du cylindre,
    l'agencement étant tel que, en fonction de la position relative de la paroi de fermeture (52) par rapport à la face d'extrémité (59) du porte-membrane (53), une dépression variable peut être établie dans l'espace entre la paroi de fermeture (52) et la membrane (54) et peut être appliquée à un côté de la membrane (54), dépression qui, en coopération avec la dépression régnant dans la capacité (60), déplace la membrane (54) vers l'orifice central (58) et ferme ainsi cet orifice, ou écarte la membrane de l'orifice central (58) et découvre ainsi cet orifice,
    caractérisé en ce que
    le cylindre circulaire creux (51) est maintenu sur le porte-membrane (53) de manière qu'il puisse être déplacé en va-et-vient en direction longitudinale,
    la membrane (54) est étanchée vis-à-vis de la paroi cylindrique interne du cylindre creux (51) déplaçable en va-et-vient, et est fixée au porte-membrane (53),
    la membrane (54) est disposée au-dessus de la face d'extrémité (59) du porte-membrane (53), face qui présente l'orifice central (58) et au moins un orifice supplémentaire (63, 64, 65), de manière qu'au moins un orifice supplémentaire ne soit pas recouvert par la membrane (54) lorsque celle-ci ferme l'orifice central (58).
  2. Dispositif de raccordement selon la revendication 1, caractérisé en ce que le porte-membrane (53) est relié au cylindre creux (51) par un assemblage à vis (55, 56).
  3. Dispositif de raccordement selon la revendication 2, caractérisé en ce que l'assemblage à vis est formé par au moins un tenon (55) prévu sur le porte-membrane (53) et engagé dans un évidement hélicoïdal (56) ménagé dans la paroi du cylindre creux.
  4. Dispositif de raccordement selon la revendication 1, caractérisé en ce qu'une pièce élastique de fermeture étanche (66) est placée au centre du côté intérieur de la paroi de fermeture (52) du cylindre (51).
  5. Dispositif de raccordement selon la revendication 4, caractérisé en ce que le porte-membrane est pourvu, à sa face d'extrémité supérieure (59), d'un rebord périphérique (57) qui, ensemble avec la membrane (54) et la face d'extrémité supérieure (59), délimite la capacité (60) sur les côtés.
  6. Dispositif de raccordement selon une des revendications précédentes, caractérisé en ce que
    la bouteille est une bouteille d'aspiration dans laquelle le vide a été fait préalablement,
    la capacité (60) est reliée à travers l'orifice central (58) à la bouteille d'aspiration et
    la capacité (60) est reliée à travers au moins un orifice supplémentaire (63) à la tubulure d'admission (23) pour les liquides de plaies à aspirer dans la bouteille.
  7. Dispositif de raccordement selon une des revendications précédentes, caractérisé en ce que la capacité (60) est reliée à travers un orifice de mesure (64), ménagé dans la face d'extrémité supérieure (59), à une tubulure (61) pour le raccordement d'un indicateur de vide.
  8. Dispositif de raccordement selon une des revendications précédentes, caractérisé en ce que la capacité (60) est reliée à travers un orifice de déversement (65) à une tubulure de déversement (62) pour un récipient de déversement à raccorder.
EP92104631A 1987-01-20 1988-01-19 Connecteur pour bouteille d'aspiration de fluides de blessures Expired - Lifetime EP0494089B1 (fr)

Applications Claiming Priority (9)

Application Number Priority Date Filing Date Title
DE3701386 1987-01-20
DE3701386 1987-01-20
DE3711093 1987-04-02
DE3711093 1987-04-02
DE3724483A DE3724483C2 (de) 1987-01-20 1987-07-24 Vorevakuierbare Saugflasche zum Absaugen von Wundflüssigkeiten
DE3724483 1987-07-24
DE8714456U DE8714456U1 (fr) 1987-10-30 1987-10-30
DE8714456U 1987-10-30
EP88900811A EP0343168B1 (fr) 1987-01-20 1988-01-19 Dispositif pour aspirer les fluides des blessures

Related Parent Applications (2)

Application Number Title Priority Date Filing Date
EP88900811.6 Division 1988-01-19
EP88900811A Division EP0343168B1 (fr) 1987-01-20 1988-01-19 Dispositif pour aspirer les fluides des blessures

Publications (2)

Publication Number Publication Date
EP0494089A1 EP0494089A1 (fr) 1992-07-08
EP0494089B1 true EP0494089B1 (fr) 1998-07-08

Family

ID=27433800

Family Applications (2)

Application Number Title Priority Date Filing Date
EP92104631A Expired - Lifetime EP0494089B1 (fr) 1987-01-20 1988-01-19 Connecteur pour bouteille d'aspiration de fluides de blessures
EP88900811A Expired - Lifetime EP0343168B1 (fr) 1987-01-20 1988-01-19 Dispositif pour aspirer les fluides des blessures

Family Applications After (1)

Application Number Title Priority Date Filing Date
EP88900811A Expired - Lifetime EP0343168B1 (fr) 1987-01-20 1988-01-19 Dispositif pour aspirer les fluides des blessures

Country Status (6)

Country Link
US (1) US5073172A (fr)
EP (2) EP0494089B1 (fr)
JP (1) JP2739761B2 (fr)
AT (2) ATE87838T1 (fr)
DE (2) DE3856215D1 (fr)
WO (1) WO1988005319A1 (fr)

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Publication number Publication date
DE3880129D1 (de) 1993-05-13
US5073172A (en) 1991-12-17
ATE87838T1 (de) 1993-04-15
JP2739761B2 (ja) 1998-04-15
EP0494089A1 (fr) 1992-07-08
WO1988005319A1 (fr) 1988-07-28
EP0343168A1 (fr) 1989-11-29
ATE168016T1 (de) 1998-07-15
JPH02502609A (ja) 1990-08-23
EP0343168B1 (fr) 1993-04-07
DE3856215D1 (de) 1998-08-13

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